Senior Automation Engineer
@ Long Finch TechnologiesSenior Automation Engineer
About the job
A biopharma company seeks an experienced automation engineer to support DeltaV systems in manufacturing, ensuring GMP compliance and solving issues during plant execution.
Requirements
- DeltaV DCS automation experience
- Troubleshooting skills
- Support C&Q activities
- Regulatory knowledge
Qualifications
- 12+ years experience
- Onsite support
- Mentorship skills
- GMP understanding
Full job description
Job Description:
· Role requires a senior level automation engineer comfortable operating independently while supporting others.
· No CSV authorship responsibility: CSV activities are supported indirectly through automation execution and issue resolution.
· DeltaV DCS automation experience in pharmaceutical / biopharma manufacturing (DeltaV Batch experience is a must, not Continuous DeltaV)
· Strong troubleshooting and problem solving skills in live manufacturing environments, including commissioning, issue triage, and rapid resolution under GMP constraints
· Deep understanding of biopharma regulatory expectations (GMP, validation, ISA 88, GAMP) and ability to apply them during real time plant execution
JD:
· Serve as an onsite DeltaV Automation Engineer supporting C&Q execution activities.
· Work independently to troubleshoot, configure, and support DeltaV control system logic, phases, and automation components during C&Q.
· Provide technical mentorship and guidance to junior engineers and intermediate engineers, answering questions and supporting issue resolution in real time.
· Support C&Q activities including test execution support, issue investigation, remediation, and re test preparation related to automation scope.
· Collaborate closely with Cognizant and client teams onsite to ensure automation behavior aligns with approved Functional Specifications and test expectations.
· Respond to automation related questions arising during commissioning and qualification activities.
· Identify automation issues, propose technical solutions, and support implementation under change control where required.
· Maintain compliance with applicable GMP requirements and site procedures during onsite execution.
· Years of Experience: 12.00 Years of Experience
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